CN102605461A - Method for preparing protein/polyving akohol composite fiber by utilizing polybasic carboxylic acid as cross linking agent - Google Patents
Method for preparing protein/polyving akohol composite fiber by utilizing polybasic carboxylic acid as cross linking agent Download PDFInfo
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Abstract
The invention discloses a method for preparing protein/polyving akohol composite fiber by utilizing polybasic carboxylic acid as a cross linking agent, which is characterized by comprising the following steps of: uniformly mixing 5-8 parts by weight of protein, 15-26.5 parts by weight of polyving akohol and 0.8-2 parts by weight of polybasic carboxylic acid cross linking agent in a mixer; adding into 66.5-79.2 parts by weight of deionized water; dissolving for 3-8h at the temperature of 90-98 DEG C, preparing spinning solution; preparing nascent fiber through wet spinning; after drying the nascent fiber, carrying out heat stretching and heat shaping; in a heat stretching and heat shaping process, enabling a system to form a cross linking structure by the organic polybasic carboxylic acid cross linking agent; fixing the protein in the fiber through chemical crosslinking; carrying out acetalation processing according to a short fiber acetalation process and a long fiber acetalation process of common vinylon; rinsing, oiling, crimping, cutting and drying the processed fiber; and preparing the protein/polyving akohol composite fiber with required specification.
Description
Technical field
The present invention relates to a kind of method for preparing protein/polyvinyl alcohol composite fiber with polybasic carboxylic acid as crosslinking agent.The manufacturing field that belongs to the protein function fiber.
Background context
Native protein is that nature offers human extremely valuable thing, and to its very big application prospect that is used, its fiber is comfortable, soft, easy dyeing with fiber condition.But pure azelon fibre forming property is poor, intensity is low, difficulty in spinning.And the polyvinyl alcohol good spinnability, the fiber after spinning, heat treatment and acetalation has higher-strength, ABRASION RESISTANCE and hygroscopicity.Remedy shortcomings such as the polyvinyl alcohol dyeability is poor, elastic recovery rate is low with protein and polyvinyl alcohol are compound, combined spinnability, ABRASION RESISTANCE, high strength and the hygroscopicity of skin-friendly, easy dyeing property and the polyvinyl alcohol of protein simultaneously.
There are various plants albumen and animal protein to be used to carry out the research and development of co-blended spinning at present, as in the Chinese patent 200410042731.9,01104271.0,01106274.6,90106200.6 preparation method with the composite fibre of rapeseed protein, soybean protein isolate, milk protein, silk-fibroin and polyvinyl alcohol being provided respectively with polyvinyl alcohol.The protein composite fiber function is many, purposes is wide, and have skin-friendly, gas permeability and lead moistly as taking clothing that fiber production goes out, be one type of fiber that dress is very comfortable; Have dyeability, anti-flammability and comfortableness preferably as the artificial hair goods; In addition protein composite fiber with its outstanding human body compatibility in field of biomedical materials by broad research; Chinese patent CN101187089A discloses the preparation method of a kind of fibroin albumen and polyvinyl alcohol blending antibacterial nanometer fiber, and this fiber can be used as the fibre for tissue engineering scaffold material.
Protein and polyvinyl alcohol blending belong to the incompatible system of thermodynamics; Simple protein and the placement for a long time of polyvinyl alcohol blending spinning solution can be separated; Therefore needing to add crosslinking agent carries out crosslinked to two components; Improve its compatibility, various albumen/polyvinyl alcohol composite fibers protein in use and washing process very easily runs off simultaneously, therefore also need albumen " be fixed " on the polyvinyl alcohol strand through crosslinking agent.Chinese patent 200510020902 discloses a kind ofly does the method for crosslinking agent modified collagen albumen-polyvinyl alcohol composite fiber with metal ion, is on the basis of containing collagen and polyvinyl alcohol, has added the metal ion of chelating crosslinked action; The composite fibre of preparation not only intensity is high; And protein content is high, is evenly distributed, and dyeability is good; Production cost is low, and has certain antimildew and antibacterial effect.Belong to the physical crosslinking effect but the chelating of metal ion is crosslinked, crosslinked poor stability, collagen runs off easily in fiber last handling process and the use.Chinese patent CN1234926C discloses a kind of preparation method of plant protein synthetic fiber; To prepare viscosity be 120～400 seconds spinning solution through in spinning solution, adding boric acid, borax or sodium phosphate; The fiber good permeability that makes; Skin-friendly is good, but boric acid, borax or sodium phosphate can only play complexing, and is very poor to the fixed effect of albumen.Chinese patent CN100558957C discloses a kind of method for preparing collagen/polyvinyl alcohol composite fiber with glutaraldehyde as crosslinking agent; Be respectively to be dissolved in deionized water by finite concentration collagen, polyvinyl alcohol and glutaraldehyde; Again collagen solution is dispersed in the poly-vinyl alcohol solution; Regulate pH=5～11 backs with acid or alkali and add glutaraldehyde solutions and form spinning solutions, through wet spinning, solidify, post processing obtains collagen/polyvinyl alcohol composite fiber.Wherein, glutaraldehyde can effectively " be fixed " protein through chemical bonding crosslinked with collagen albumen and polyvinyl alcohol, and not only intensity is high for the fiber that obtains, protein content is high, and hot water resistance is good, and dyeability is good.But glutaraldehyde has certain bio-toxicity; In the preparation of fiber and use, all be unfavorable for health; Simultaneously in the formal process, the crosslinking points that glutaraldehyde forms in the fiber very easily ruptures under acid condition, causes that protein runs off in a large number in the fiber formalizing process.
Summary of the invention
The objective of the invention is to the deficiency of prior art and a kind of method for preparing protein/polyvinyl alcohol composite fiber with polybasic carboxylic acid as crosslinking agent is provided.Be characterized in: spinning solution comprises water, protein, polyvinyl alcohol and organic spinning solution how far mixing of carboxylic acid crosslinking agent forms, and processes as-spun fibre through wet spinning, makes finished fiber through steps such as hot-stretch, HEAT SETTING and acetalations again.Technology is simple to operation, adopts the organic polycarboxylic acid compounds to make crosslinking agent, inanimate object toxicity, and belong to the chemical crosslinking effect, and crosslinking chemical bond is ester bond or amido link, and crosslinking points is stable under the strong acidic condition that acetalation is bathed, and cross-linking effect is good.
The object of the invention is realized that by following technical measures wherein said raw material umber is parts by weight except that specified otherwise.
Preparation method with polycarboxylic acid crosslinked protein/polyvinyl alcohol composite fiber comprises following steps:
(1) preparation of protein/polyvinyl alcohol composite spinning stoste
With protein 5～18 weight portions, polyvinyl alcohol 15～26.5 weight portions, polycarboxylic acid crosslinked dose 0.8～2 weight portion adds in 66.5～79.2 parts by weight of deionized water, and under agitation, in 90～98 ℃ of temperature, dissolving 3～8h makes spinning solution;
(2) wet spinning of stoste
With spinning solution pressure filtration, deaeration, 60～90 ℃ of temperature through measuring pump, filter, the wet spinning spinning head of the 0.06～0.4mm ejection from the aperture, dynamic analysis of spinning is coagulation forming in coagulating bath, and carries out making as-spun fibre after 1～6 times hygrometric state stretches;
(3) post processing of as-spun fibre
Need carry out hot-stretch and HEAT SETTING after the as-spun fibre drying handles; 2～8 times of hot-stretchs; 180～230 ℃ of hot-stretch temperature, 170～220 ℃ of heat setting temperatures, heat-setting time 2～15min; The organic polycarboxylic acid crosslinking agent at high temperature makes system form cross-linked structure in hot-stretch and the HEAT SETTING process, and protein is fixed in the fiber through chemical crosslinking.The fiber that heat treatment finishes carries out acetalation to be handled; Acetalation is handled and is undertaken by the short fiber acetalation technology or the long filament acetalation technology of common polyvinyl; Fiber after the processing through washing, oiling, curl, cut off, dry, makes the protein/polyvinyl alcohol composite fiber of required specification again;
Wherein, the polyvinyl alcohol degree of polymerization 1700～2600, alcoholysis degree is greater than 99%.
Protein is any in cottonseed protein, rapeseed protein, peanut protein or the soybean protein in the vegetable protein; In collagen in the animal protein, milk protein, silk-fibroin, pupa albumen or the keratin etc. any.
Polycarboxylic acid crosslinked dose is poly, citric acid, 1,2,3-tricarboxylic acids propane or 1,2,3, any in the 4-tetrabasic carboxylic acid butane.
Spinning coagulation bath is 30～50 ℃ of temperature, pH value 2～7, and the sodium sulphate-aqueous sulfuric acid of proportion 1.29～1.35 transfers to the pH value of coagulating bath according to the protein of being selected for use the isoelectric point of this protein;
Hydroformylation liquid is formaldehyde 25～60g/L, sulfuric acid 120～250g/L, sodium sulphate 200～360g/L, 50～75 ℃ of hydroformylation temperature, hydroformylation time 10～25min.
Protein/polyvinyl alcohol composite fiber can be used for dress ornament textiles, artificial hair, operation suture thread, hospital gauze etc.
Performance test:
Fiber linear density is tested by GB GB/T 14335-2008 " staple line density test method ".Fibrous mechanical property is tested according to GB GB/T 14337-2008 " staple fibre Erichsen test method ".Protein loss rate is measured through triumphant formula nitriding in the fiber of formal front and back.The Rp value is a fiber when in water, heating up with 2 ℃/min under the load of 0.001cN/dtex, and fibre length is shunk 20% o'clock corresponding water temperature;
The result shows that the line density of this protein/polyvinyl alcohol composite fiber is 1～120dtex, and fracture strength is 1～5cN/dtex, and elongation at break is 10～30%, and protein loss rate is less than 10% in the formalizing process, and the Rp value is 95～115 ℃.
The present invention has following advantage:
1. used crosslinking agent is the polybasic carboxylic acid class, inanimate object toxicity, and the protein/polyvinyl alcohol composite fiber that makes has excellent biological compatibility, can be used for the preparation of medical material and underclothes.
2. polybasic carboxylic acid adds in spinning solution, but its cross-linking reaction occurs in the fiber last handling process, therefore in stoste, add crosslinking agent after, former fluid viscosity does not change thereupon, the wet spinning process can not be affected.
3. the pH value through regulating coagulating bath has further promoted the coagulation forming of fiber about the isoelectric point of selecting for use protein, and the coagulating bath of acidity helps to be suppressed at the stripping of polybasic carboxylic acid in the strand process of setting.
4. make crosslinking agent with polybasic carboxylic acid; Protein and polyvinyl alcohol have new covalent bond production, in conjunction with bond energy bigger, protein be difficult for to run off; The addition of protein is bigger, and protein/polyvinyl alcohol composite fiber has higher intensity when having than high nitrogen content.
5. it is extensive that composite fibre prepares in the process protein source, and molecular weight ranges is big, can select for use flexibly as required, helps suitability for industrialized production.
6. composite fibre has good snugness of fit, dyeability is good, wrinkle resistance is strong, and health care and medical functions are also arranged simultaneously, can be used for high-grade dress ornament textiles, senior wig, exempts to tear open operation suture thread etc.
7. the preparation of composite fibre does not have specific (special) requirements to equipment, adopts wet spinning, and simple to operate, technical maturity can be realized fiber production on existing polyvinyl spinning equipment, reduce cost.
The specific embodiment
Through instance the present invention is specifically described below.Be necessary to be pointed out that at this; Following instance only is used for the present invention is further specified; Can not be interpreted as the restriction to protection domain of the present invention, the person skilled in the art in this field can make some nonessential improvement and adjustment to the present invention according to the foregoing invention content.
Embodiment 1
With keratin (about isoelectric point 4.5) 5 weight portions, polyvinyl alcohol 1,799 26.5 weight portions, poly 2 weight portions, add in 66.5 parts by weight of deionized water, under agitation, in 92 ℃ of temperature, dissolving 8h makes spinning solution; With the above-mentioned spinning solution that obtains filter, after the deaeration in the spinneret orifice ejection of 90 ℃ of via hole diameter 0.4mm of temperature, be coagulation forming in sodium sulphate-sulfuric acid coagulating bath of 4.5 in 45 ℃ of temperature, proportion 1.29, pH value, the hygrometric state stretching obtains as-spun fibre for 2 times.After the as-spun fibre drying 225 ℃ of temperature stretch 2 times, at 220 ℃ of HEAT SETTING 8min of temperature; The fiber that heat treatment finishes is through long filament acetalation PROCESS FOR TREATMENT; The hydroformylation formula of liquid is formaldehyde 40g/L, sulfuric acid 250g/L, sodium sulphate 270g/L; 75 ℃ of hydroformylation temperature, hydroformylation time 25min, then fiber obtains finished fiber after washing, oil, drying.The fiber number of the finished fiber that obtains is 115dtex, and fracture strength is 2.5cN/dtex, and elongation at break is 20.3%, and softening point in water is 108 ℃, and the fibrin turnover rate is 2.3% in the acetalation process.This kind keratin/polyvinyl alcohol composite fiber can be used as wig fiber etc. and uses.
Embodiment 2
With milk protein (about isoelectric point 4.1) 8 weight portions, polyvinyl alcohol 2,699 16 weight portions, citric acid 1.2 weight portions, add in 74.8 parts by weight of deionized water, under agitation, in 98 ℃ of temperature, dissolving 4h makes spinning solution; With the above-mentioned spinning solution that obtains filter, after the deaeration in the spinneret orifice ejection of 65 ℃ of via hole diameter 0.06mm of temperature, be coagulation forming in sodium sulphate-sulfuric acid coagulating bath of 4.1 in 42 ℃ of temperature, proportion 1.32, pH value, the hygrometric state stretching obtains as-spun fibre for 2 times.After the as-spun fibre drying 220 ℃ of temperature stretch 3 times, at 210 ℃ of HEAT SETTING 2min of temperature; The fibre cutting that heat treatment finishes is after short fiber acetalation PROCESS FOR TREATMENT; The hydroformylation formula of liquid is formaldehyde 45g/L, sulfuric acid 240g/L, sodium sulphate 200g/L; 65 ℃ of hydroformylation temperature, hydroformylation time 15min, then fiber obtains finished fiber after washing, oil, drying.The fiber number of the finished fiber that obtains is 1.2dtex, and fracture strength is 3.5cN/dtex, and elongation at break is 17.4%, and softening point in water is 112 ℃, fibrin turnover rate 5.7% in the acetalation process.This kind milk protein/polyvinyl alcohol composite fiber can be used as to be taken fiber etc. and uses.
Embodiment 3
With rapeseed protein (about isoelectric point 5) 5 weight portions, polyvinyl alcohol 2,099 15 weight portions, 1,2,3,4-tetrabasic carboxylic acid butane 0.8 weight portion adds in 79.2 parts by weight of deionized water, and under agitation, in 92 ℃ of temperature, dissolving 3h makes spinning solution; With the above-mentioned spinning solution that obtains filter, after the deaeration in the spinneret orifice ejection of 60 ℃ of via hole diameter 0.08mm of temperature, be coagulation forming in sodium sulphate-sulfuric acid coagulating bath of 5 in 50 ℃ of temperature, proportion 1.34, pH value, the hygrometric state stretching obtains as-spun fibre for 4 times.After the as-spun fibre drying 200 ℃ of temperature stretch 2 times, at 190 ℃ of HEAT SETTING 5min of temperature; The fiber that heat treatment finishes is through long filament acetalation PROCESS FOR TREATMENT; The hydroformylation formula of liquid is formaldehyde 60g/L, sulfuric acid 200g/L, sodium sulphate 220g/L; 65 ℃ of hydroformylation temperature, hydroformylation time 12min, then fiber obtains finished fiber after washing, oil, curl, cut off, drying.The fiber number of the finished fiber that obtains is 1.3dtex, and fracture strength is 3.1cN/dtex, and elongation at break is 16.7%, and softening point in water is 108 ℃, and the fibrin turnover rate is 4.7% in the acetalation process.This kind rapeseed protein/polyvinyl alcohol composite fiber can be used as to be taken fiber etc. and uses.
Embodiment 4
With soybean protein (about isoelectric point 4.6) 10 weight portions, polyvinyl alcohol 2,099 20 weight portions, 1,2,3-tricarboxylic acids propane 1.8 weight portions add in 68.2 parts by weight of deionized water, and under agitation, in 90 ℃ of temperature, dissolving 5h makes spinning solution; With the above-mentioned spinning solution that obtains filter, after the deaeration in the spinneret orifice ejection of 70 ℃ of via hole diameter 0.1mm of temperature, be coagulation forming in sodium sulphate-sulfuric acid coagulating bath of 4.6 in 40 ℃ of temperature, proportion 1.35, pH value, the hygrometric state stretching obtains as-spun fibre for 2 times.After the as-spun fibre drying 230 ℃ of temperature stretch 8 times, at 180 ℃ of HEAT SETTING 10min of temperature; The fiber that heat treatment finishes is through long filament acetalation PROCESS FOR TREATMENT; The hydroformylation formula of liquid is formaldehyde 40g/L, sulfuric acid 220g/L, sodium sulphate 260g/L; 70 ℃ of hydroformylation temperature, hydroformylation time 15min, then fiber obtains finished fiber after washing, oil, curl, cut off, drying.The fiber number of the finished fiber that obtains is 1.5dtex, and fracture strength is 3.7cN/dtex, and elongation at break is 15.6%, and softening point in water is 114 ℃, and the fibrin turnover rate is 7.3% in the acetalation process.This kind soybean protein/polyvinyl alcohol composite fiber can be used as to be taken fiber etc. and uses.
Embodiment 5
With collagen (about isoelectric point 5.3) 18 weight portions, polyvinyl alcohol 2,499 18 weight portions, citric acid 1.8 weight portions, add in 68.2 parts by weight of deionized water, under agitation, in 95 ℃ of temperature, dissolving 5h makes spinning solution; With the above-mentioned spinning solution that obtains filter, after the deaeration in the spinneret orifice ejection of 65 ℃ of via hole diameter 0.25mm of temperature, be 1.30 at 30 ℃ of temperature, proportion, pH value is a coagulation forming in sodium sulphate-sulfuric acid coagulating bath of 5.3, the hygrometric state stretching obtains as-spun fibre for 1 times.After the as-spun fibre drying 180 ℃ of temperature stretch 2 times, at 170 ℃ of HEAT SETTING 15min of temperature; The fiber that heat treatment finishes is through long filament acetalation PROCESS FOR TREATMENT; The hydroformylation formula of liquid is formaldehyde 25g/L, sulfuric acid 120g/L, sodium sulphate 360g/L; 50 ℃ of hydroformylation temperature, hydroformylation time 10min, then fiber obtains finished fiber after washing, oil, drying.The fiber number of the finished fiber that obtains is 87.6dtex, and fracture strength is 1.9cN/dtex, and elongation at break is 25.3%, and softening point in water is 98 ℃, and the fibrin turnover rate is 8.7% in the acetalation process.This kind collagen/polyvinyl alcohol composite fiber can be used as wig fiber etc. and uses.
Claims (5)
1. prepare the method for protein/polyvinyl alcohol composite fiber with polybasic carboxylic acid as crosslinking agent, it is characterized in that this method may further comprise the steps:
(1) preparation of protein/polyvinyl alcohol composite spinning stoste
With protein 5～18 weight portions, polyvinyl alcohol 15～26.5 weight portions, polycarboxylic acid crosslinked dose 0.8～2 weight portion adds in 66.5～79.2 parts by weight of deionized water, and under agitation, in 90～98 ℃ of temperature, dissolving 3～8h makes spinning solution;
(2) wet spinning of stoste
With spinning solution pressure filtration, deaeration, 60～90 ℃ of temperature through measuring pump, filter, the wet spinning spinning head of the 0.06～0.4mm ejection from the aperture, dynamic analysis of spinning is coagulation forming in coagulating bath, and carries out making as-spun fibre after 1～6 times hygrometric state stretches;
(3) post processing of as-spun fibre
Need carry out hot-stretch and HEAT SETTING after the as-spun fibre drying handles; 2～8 times of hot-stretchs; 180～230 ℃ of hot-stretch temperature, 170～220 ℃ of heat setting temperatures, heat-setting time 2～15min; The organic polycarboxylic acid crosslinking agent at high temperature makes system form cross-linked structure in hot-stretch and the HEAT SETTING process, and protein is fixed in the fiber through chemical crosslinking; The fiber that heat treatment finishes carries out acetalation to be handled; Acetalation is handled and is undertaken by the short fiber acetalation technology or the long filament acetalation technology of common polyvinyl; Fiber after the processing through washing, oiling, curl, cut off, dry, makes the protein/polyvinyl alcohol composite fiber of required specification again;
Wherein, the polyvinyl alcohol degree of polymerization 1700～2600, alcoholysis degree is greater than 99%.
2. prepare the method for protein/polyvinyl alcohol composite fiber with polybasic carboxylic acid as crosslinking agent according to claim 1, it is characterized in that protein is any in the cottonseed protein, rapeseed protein, peanut protein, soybean protein in the vegetable protein; Perhaps any in the collagen in the animal protein, milk protein, silk-fibroin, pupa albumen, the keratin.
3. prepare the method for protein/polyvinyl alcohol composite fiber with polybasic carboxylic acid as crosslinking agent according to claim 1, it is characterized in that polycarboxylic acid crosslinked dose is poly, citric acid, 1,2; 3-tricarboxylic acids propane or 1; 2,3, any in the 4-tetrabasic carboxylic acid butane.
4. the method for preparing protein/polyvinyl alcohol composite fiber according to claim 1 with polybasic carboxylic acid as crosslinking agent; It is characterized in that spinning coagulation bath is 30～50 ℃ of temperature; The aqueous sodium persulfate solution of proportion 1.29～1.35 transfers to the pH value of coagulating bath according to the protein of being selected for use the isoelectric point of this protein.
5. the method for preparing protein/polyvinyl alcohol composite fiber according to claim 1 with polybasic carboxylic acid as crosslinking agent; It is characterized in that this hydroformylation liquid is formaldehyde 25～60g/L, sulfuric acid 120～250g/L, sodium sulphate 200～360g/L; 50～75 ℃ of hydroformylation temperature, hydroformylation time 10～25min.
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| CN102797072A (en) * | 2012-07-27 | 2012-11-28 | 安徽绿朋实业有限公司 | Novel vinylon-based home textile fiber and preparation method thereof |
| CN102978739A (en) * | 2012-12-25 | 2013-03-20 | 四川大学 | Preparation method of polyethylene glycol/polyvinyl alcohol phase change energy storage fiber by in situ crosslinking |
| CN103436986A (en) * | 2013-08-01 | 2013-12-11 | 湖州珠力纳米材料科技开发有限公司 | Preparation method of polypeptide soybean protein complex fiber |
| CN104372439A (en) * | 2014-11-10 | 2015-02-25 | 苏州蔻美新材料有限公司 | Bio-based protein composite fiber and preparation method thereof |
| CN105350178A (en) * | 2015-11-20 | 2016-02-24 | 苏州大学 | Polyvinyl alcohol/ animal milk nanofiber membrane and preparation method thereof |
| CN106511252A (en) * | 2016-12-28 | 2017-03-22 | 芜湖凯奥尔环保科技有限公司 | Cow milk mask containing traditional Chinese medicine content and preparation method thereof |
| CN109509902A (en) * | 2018-10-17 | 2019-03-22 | 盐城工业职业技术学院 | A kind of preparation method of PVA-KN type dyeing conductive film |
| CN110655795A (en) * | 2019-10-25 | 2020-01-07 | 仲恺农业工程学院 | Cottonseed protein/PVA composite membrane and preparation method thereof |
| CN113249822A (en) * | 2021-05-30 | 2021-08-13 | 天元纤维股份有限公司 | Milk velvet and preparation method thereof |
| CN115151235A (en) * | 2020-01-21 | 2022-10-04 | 纽泰克温图斯公司 | Continuous production of keratin fibers |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102797072A (en) * | 2012-07-27 | 2012-11-28 | 安徽绿朋实业有限公司 | Novel vinylon-based home textile fiber and preparation method thereof |
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| CN109509902A (en) * | 2018-10-17 | 2019-03-22 | 盐城工业职业技术学院 | A kind of preparation method of PVA-KN type dyeing conductive film |
| CN110655795A (en) * | 2019-10-25 | 2020-01-07 | 仲恺农业工程学院 | Cottonseed protein/PVA composite membrane and preparation method thereof |
| CN115151235A (en) * | 2020-01-21 | 2022-10-04 | 纽泰克温图斯公司 | Continuous production of keratin fibers |
| CN113249822A (en) * | 2021-05-30 | 2021-08-13 | 天元纤维股份有限公司 | Milk velvet and preparation method thereof |
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